# Takotsubo Syndrome Following Inhalation of K4: A Case Report

**Authors:** Leandro M Valente, Gabrielle Santos, Ricardo Velho, José Filipe Santos, Inês Gonçalves, Pedro D Lopes, Mariana Guerra, Lurdes M Correia

PMC · DOI: 10.7759/cureus.102819 · Cureus · 2026-02-02

## TL;DR

A 59-year-old man developed Takotsubo syndrome after inhaling K4, a synthetic cannabinoid, highlighting a rare but serious health risk.

## Contribution

This case report links inhaled synthetic cannabinoid K4 to Takotsubo syndrome as a novel trigger.

## Key findings

- The patient exhibited severe left ventricular dysfunction consistent with Takotsubo syndrome.
- No significant coronary artery disease was found, supporting a non-ischemic cause.
- Inhaled K4 was identified as the most likely trigger after excluding other potential causes.

## Abstract

Takotsubo syndrome (TS), also known as stress cardiomyopathy, is a clinical condition characterized by transient left ventricular dysfunction in the absence of coronary artery disease findings. The most widely accepted mechanism suggests a trigger, either physical or emotional stress, which causes catecholamine release and results in myocardial stunning and contractility alterations. Clinically and analytically, it can mimic acute coronary syndromes. Synthetic cannabinoids, such as the inhaled drug K4, are more powerful than phytocannabinoids and act as strong agonists of cannabinoid receptors, stimulating the sympathetic nervous system, which can serve as a trigger for TS. We report a case of a 59-year-old man with a personal history of schizophrenia and drug addiction, admitted to the emergency room for severe dyspnea and psychomotor agitation. Prior to the onset of symptoms, he had reportedly used the inhaled drug K4. Due to markedly elevated high-sensitivity troponin I and electrocardiographic changes suggestive of myocardial ischemia, an echocardiogram was performed, revealing severe left ventricular dysfunction with mid-apical akinesia of all cardiac walls. Cardiac catheterization showed no significant coronary disease. The patient was diagnosed with TS. After excluding other potential triggers, the use of inhaled K4 was considered the most likely trigger for TS.

## Linked entities

- **Chemicals:** K4 (PubChem CID 5487705)
- **Diseases:** schizophrenia (MONDO:0005090), Takotsubo syndrome (MONDO:0019018)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CNR2 (cannabinoid receptor 2) [NCBI Gene 1269] {aka CB-2, CB2, CX5}, CNR1 (cannabinoid receptor 1) [NCBI Gene 1268] {aka CANN6, CB-R, CB1, CB1A, CB1K5, CB1R}
- **Diseases:** psychomotor agitation (MESH:D011595), drug addiction (MESH:D019966), cardiogenic shock (MESH:D012770), dyspnea (MESH:D004417), anterior fascicular block (MESH:D002037), myocardial ischemia (MESH:D017202), myocardial stunning (MESH:D017682), Poison (MESH:D011041), ischemic (MESH:D002545), asystole (MESH:D006323), cardiogenic pulmonary edema (MESH:D011654), leukocytosis (MESH:D007964), schizophrenia (MESH:D012559), metabolic acidosis (MESH:D000138), ventricular dysfunction (MESH:D018754), shock (MESH:D012769), head trauma (MESH:D006259), death (MESH:D003643), acute coronary syndrome (MESH:D054058), neutrophilia (MESH:C563010), Gebrochenes-Herz syndrome (MESH:D013577), TS (MESH:D054549), coronary disease (MESH:D003327), hypotension (MESH:D007022), hearing loss (MESH:D034381), prolonged QTc interval (MESH:D008133), ARDS (MESH:D012128), cognitive decline (MESH:D003072), mitral insufficiency (MESH:D008944), burns (MESH:D002056), non (MESH:C580335), hypoxemia (MESH:D000860), left ventricular dysfunction (MESH:D018487), respiratory failure (MESH:D012131), ventricular arrhythmias (MESH:D001145), heart failure (MESH:D006333), tachycardia (MESH:D013610), cardiomyopathy (MESH:D009202), ventricular wall rupture (MESH:D006341), akinesia (MESH:C537921), coronary artery disease (MESH:D003324), allergies (MESH:D004342), cardiac injury (MESH:D006331)
- **Chemicals:** lactate (MESH:D019344), catecholamine (MESH:D002395), K4 (MESH:C048655), delta-9 THC (MESH:D013759), HCO3 (MESH:D001639), N-terminal pro-brain natriuretic peptide (-), clozapine (MESH:D003024), oxygen (MESH:D010100), norepinephrine (MESH:D009638), cannabinoid (MESH:D002186)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12958257/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12958257/full.md

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Source: https://tomesphere.com/paper/PMC12958257